Canonical Allele Identifier: CA9359330

Gene: CEP89

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32918279C>T , CM000681.2:g.32918279C>T	GRCh38
NC_000019.9:g.33409185C>T , CM000681.1:g.33409185C>T	GRCh37
NC_000019.8:g.38101025C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305768.10:c.1329G>A MANE Select	ENSP00000306105.4:p.Gln443=
ENST00000305768.9:c.1329G>A	ENSP00000306105.4:p.Gln443=
ENST00000586984.6:c.1225G>A	ENSP00000465141.1:p.Val409Ile
ENST00000591698.5:c.1185G>A	ENSP00000467544.1:n.1185G>A
NM_032816.4:c.1329G>A	NP_116205.3:p.Gln443=
XM_005259344.2:c.1225G>A	XP_005259401.1:p.Val409Ile
XM_005259346.2:c.1329G>A	XP_005259403.1:p.Gln443=
XM_011527425.1:c.588G>A	XP_011525727.1:p.Gln196=
XR_935866.1:n.1375G>A
XM_005259344.3:c.1225G>A	XP_005259401.1:p.Val409Ile
XM_017027398.1:c.1329G>A	XP_016882887.1:p.Gln443=
XM_024451745.1:c.588G>A	XP_024307513.1:p.Gln196=
XR_002958372.1:n.1479G>A
XR_935866.2:n.1375G>A
NM_032816.5:c.1329G>A MANE Select	NP_116205.3:p.Gln443=